Control Units

GUDID 00887761974272

Sensor Control FloatLine

TRUMPF Medizin Systeme GmbH + Co. KG

Operating room equipment remote control
Primary Device ID00887761974272
NIH Device Record Key42838fc1-6314-43e9-a849-65b43e038fc6
Commercial Distribution StatusIn Commercial Distribution
Brand NameControl Units
Version Model Number1808992
Company DUNS330961223
Company NameTRUMPF Medizin Systeme GmbH + Co. KG
Device Count1
DM Exemptfalse
Pre-market Exempttrue
MRI Safety StatusLabeling does not contain MRI Safety Information
Human Cell/Tissue Productfalse
Device Kitfalse
Device Combination Productfalse
Single Usefalse
Lot Batchfalse
Serial Numbertrue
Manufacturing Datetrue
Expiration Datefalse
Donation Id Numberfalse
Contains Natural Rubber Latexfalse
Labeled No Natural Rubber Latexfalse
RX Perscriptionfalse
OTC Over-The-Counterfalse

Customer Support Contacts

Phone+4936715860
EmailSURGICAL@HILLROM.COM
Phone+4936715860
EmailSURGICAL@HILLROM.COM
Phone+4936715860
EmailSURGICAL@HILLROM.COM
Phone+4936715860
EmailSURGICAL@HILLROM.COM
Phone+4936715860
EmailSURGICAL@HILLROM.COM
Phone+4936715860
EmailSURGICAL@HILLROM.COM

Device Identifiers

Device Issuing AgencyDevice ID
GS100887761974272 [Primary]

FDA Product Code

KXJTable, radiologic

Sterilization

Steralize Prior To Usefalse
Device Is Sterilefalse

Device Entry Metadata

Public Version StatusNew
Device Record StatusPublished
Public Version Number1
Public Version Date2023-01-13
Device Publish Date2023-01-05

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00887761968394 - TL 5000/3000 – Surgical Light2023-01-13 TruLight 5000 / 3000 Ceiling Trio
00887761968400 - TL 5000/3000 – Surgical Light2023-01-13 TruLight 5000 / 3000 Ceiling Duo
00887761968424 - TL 5000/3000 – Surgical Light2023-01-13 TruLight 5000 / 3000 Wall
00887761968431 - TL 5000/3000 – Surgical Light2023-01-13 TruLight 5000 / 3000 Mobile
00887761968448 - TL 5000/3000 – Surgical Light2023-01-13 TruLight 5000 / 3000 Ceiling Single

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